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  • Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes

    Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
    Authors:Nandita Mukhopadhyay, University of PittsburghEleanor Feingold, University of PittsburghLina Moreno-Uribe, University of IowaGeorge Wehby, University of IowaLuz Consuelo Valencia-Ramirez, Fundación Clínica Noel; Calle 14 # 43B – 146, Medellín, Antioquia, ColombiaClaudia Restrepo P Muneton, Fundación Clínica Noel; Calle 14 # 43B – 146, Medellín, Antioquia, ColombiaCarmencita Padilla, University of the PhilippinesFrederic Deleyiannis, UCHealth Medical Group, Colorado Springs, CO. USAKaare Christensen, University of Southern DenmarkFernando A Poletta, CEMIC CONICET Ctr Med Educ & Clin ResIeda M Orioli, Federal University of Rio de JaneiroJacqueline T Hecht, University of Texas Health Science Center at HoustonCarmen J Buxo, University of Puerto RicoAzeez Butali, University of IowaWasiu L Adeyemo, University of LagosAlexandre R Vieira, University of PittsburghJohn R Shaffer, University of PittsburghJeffrey C Murray, University of IowaSeth M Weinberg, University of PittsburghElizabeth Leslie, Emory UniversityMary L Marazita, University of Pittsburgh
    Date:2022
    Publisher:WILEY
    Publication Version:Author Accepted Manuscript (After Peer Review)
    License:Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

  • FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research

    FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research
    Authors:Bridget D Samuels, University of Southern CaliforniaRobert Aho, University of California San FranciscoJames F Brinkley, University of WashingtonAlejandro Bugacov, University of Southern CaliforniaEleanor Feingold, University of PittsburghShannon Fisher, Boston UniversityAna S Gonzalez-Reiche, Icahn School of Medicine at Mount SinaiJoseph G Hacia, University of Southern CaliforniaBenedikt Hallgrimsson, University of CalgaryKarissa Hansen, University of California San FranciscoMatthew P Harris, Harvard Medical SchoolThach-Vu Ho, University of Southern CaliforniaGreg Holmes, Icahn School of Medicine at Mount SinaiJoan E Hooper, University of Colorado, AuroraEthylin W Jabs, Icahn School of Medicine at Mount SinaiKenneth L Jones, University of Colorado, AuroraCarl Kesselman, University of Southern CaliforniaOphir D Klein, University of California San FranciscoElizabeth Leslie, Emory UniversityHong Li, Univ ColoradoEric C Liao, Massachusetts General HospitalHannah Long, Stanford UniversityNa Lu, Icahn School of Medicine at Mount SinaiRichard L Maas, Harvard Medical SchoolMary L Marazita, University of PittsburghJaaved Mohammed, Stanford UniversitySara Prescott, Stanford UniversityRobert Schuler, University of Southern CaliforniaLicia Selleri, University of California San FranciscoRichard A Spritz, University of Colorado, AuroraTomek Swigut, Stanford UniversityHarm van Bakel, Icahn School of Medicine at Mount SinaiAxel Visel, Lawrence Berkeley National LaboratoryIan Welsh, University of California San FranciscoCristina Williams, University of Southern CaliforniaTrevor J Williams, University of Colorado, AuroraJoanna Wysocka, Stanford UniversityYuan Yuan, University of Southern CaliforniaYang Chai, University of Southern California
    Date:2020
    Publisher:COMPANY BIOLOGISTS LTD
    Publication Version:Final Published Version

  • Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios

    Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios
    Authors:Debashree Ray, Johns Hopkins UniversitySowmya Venkataraghavan, Johns Hopkins UniversityWanying Zhang, Johns Hopkins UniversityElizabeth Leslie, Emory UniversityJacqueline B Hetmanski, Johns Hopkins UniversitySeth M Weinberg, University of PittsburghJeffrey C Murray, University of IowaMary L Marazita, University of PittsburghIngo Ruczinski, Johns Hopkins UniversityMargaret A Taub, Johns Hopkins UniversityTerri H Beaty, Johns Hopkins University
    Date:2021
    Publisher:PUBLIC LIBRARY SCIENCE
    Publication Version:Final Published Version
    License:Creative Commons Attribution 4.0 International

  • Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk

    Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk
    Authors:Elizabeth Leslie, Emory UniversityJenna C Carlson, University of PittsburghJohn R Shaffer, University of PittsburghFred Deleyiannis, UCHealth Medical GroupJacqueline T Hecht, University of Texas Health Science Center at HoustonGeorge L Wehby, University of IowaKaare Christensen, University of Southern DenmarkEleanor Feingold, University of PittsburghSeth M Weinberg, University of PittsburghMary L Marazita, University of Pittsburgh
    Date:2022
    Publisher:FRONTIERS MEDIA SA
    Publication Version:Final Published Version
    License:Creative Commons Attribution 4.0 International

  • FAT4 identified as a potential modifier of orofacial cleft laterality

    FAT4 identified as a potential modifier of orofacial cleft laterality
    Authors:Sarah W Curtis, Emory UniversityDaniel Chang, Emory UniversityMiranda R Sun, Univ WisconsinMichael Epstein, Emory UniversityJeffrey C Murray, University of IowaEleanor Feingold, University of PittsburghTerri H Beaty, Johns Hopkins Bloomberg Sch Publ HlthSeth M Weinberg, University of PittsburghMary L Marazita, University of PittsburghRobert J Lipinski, Univ WisconsinJenna C Carlson, University of PittsburghElizabeth Leslie, Emory University
    Date:2021
    Publisher:WILEY
    Publication Version:Author Accepted Manuscript (After Peer Review)

  • Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts

    Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts
    Authors:John R. Shaffer, University of PittsburghJessica LeClair, University of PittsburghJenna C. Carlson, University of PittsburghEleanor Feingold, University of PittsburghCarmen J. Buxo, University of Puerto RicoKaare Christensen, University of Southern DenmarkFrederic W. B. Deleyiannis, University of ColoradoL. Leigh Field, University of British ColumbiaJacqueline T. Hecht, University of Texas HoustonLina Moreno, University of IowaIeda M. Orioli, Federal University of Rio de JaneiroCarmencita Padilla, University of the Philippines ManilaAlexandre R. Vieira, University of PittsburghGeorge L. Wehby, University of IowaJeffrey C. Murray, University of IowaSeth M. Weinberg, University of PittsburghMary L. Marazita, University of PittsburghElizabeth Leslie, Emory University
    Date:2019
    Publisher:WILEY
    Publication Version:Author Accepted Manuscript (After Peer Review)

  • Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18

    Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18
    Authors:Huan Liu, Wuhan UniversityKaylia Duncan, University of IowaAnnika Helverson, University of IowaPriyanka Kumari, University of IowaCamille Mumm, University of IowaYao Xiao, Wuhan UniversityJenna Colavincenzo Carlson, University of PittsburghFabrice Darbellay, Lawrence Berkeley LabsAxel Visel, Lawrence Berkeley LabsElizabeth Leslie, Emory UniversityPatrick Breheny, University of IowaAlbert J. Erives, University of IowaRobert A. Cornell, University of Iowa
    Date:2020
    Publisher:ELIFE SCIENCES PUBLICATIONS LTD
    Publication Version:Final Published Version
    License:Creative Commons Attribution 4.0 International

  • Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

    Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts
    Authors:Jenna C. Carlson, University of PittsburghNichole L. Nidey, University of IowaAzeez Butali, University of IowaCarmen J. Buxo, University of Puerto RicoKaare Christensen, University of Southern DenmarkFrederic W-D Deleyiannis, University of ColoradoJacqueline T. Hecht, University of Texas HoustonL. Leigh Field, University of British ColumbiaLina M. Moreno-Uribe, University of IowaIeda M. Orioli, National Institute of Population Medical GeneticsFernando A. Poletta, National Institute of Population Medical GeneticsCarmencita Padilla, University of the PhilippinesAlexandre R. Vieira, University of PittsburghSeth M. Weinberg, University of PittsburghGeorge L. Wehby, University of IowaEleanor Feingold, University of PittsburghJeffrey C. Murray, University of IowaMary L. Marazita, University of PittsburghElizabeth Leslie, Emory University
    Date:2018
    Publisher:WILEY
    Publication Version:Author Accepted Manuscript (After Peer Review)

  • Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21

    Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21
    Authors:Nandita Mukhopadhyay, University of PittsburghMadison Bishop, Emory UniversityMichael Mortillo, Emory UniversityPankaj Chopra, Emory UniversityJacqueline B. Hetmanski, Johns Hopkins UniversityMargaret A. Taub, Johns Hopkins UniversityLina M. Moreno, University of IowaLuz Consuelo Valencia-Ramirez, Fundación Clínica NoelClaudia Restrepo, Fundación Clínica NoelGeorge L. Wehby, University of IowaJacqueline T. Hecht, University of Texas HoustonFrederic Deleyiannis, University of ColoradoAzeez Butali, University of IowaSeth M. Weinberg, University of PittsburghTerri H. Beaty, Johns Hopkins UniversityJeffrey C. Murray, University of IowaElizabeth Leslie, Emory UniversityEleanor Feingold, University of PittsburghMary L. Marazita, University of Pittsburgh
    Date:2020
    Publisher:SPRINGER
    Publication Version:Final Published Version
    License:Creative Commons Attribution 4.0 International

  • Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

    Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
    Authors:Jenna C. Carlson, University of PittsburghJennifer Standley, University of IowaAline Petrin, University of IowaJohn R Shaffer, University of PittsburghAzeez Butali, University of IowaCarmen J. Buxo, University of Puerto RicoEduardo Castilla, CEMIC: Center for Medical Education and Clinical ResearchKaare Christensen, University of Southern DenmarkFrederic W-D Deleyiannis, University of ColoradoJacqueline T. Hecht, McGovern Medical SchoolL. Leigh Field, University of British ColumbiaAriuntuul Garidkhuu, Tohoku UniversityLina M. Moreno Uribe, University of IowaNatsume Nagato, Aichi Gakuin UniversityIeda M. Orioli, National Institute of Population Medical GeneticsCarmencita Padilla, University of the Philippines ManilaFernando Poletta, CEMIC: Center for Medical Education and Clinical ResearchSatoshi Suzuki, Aichi Gakuin UniversityAlexandre R. Vieira, University of PittsburghGeorge L. Wehby, University of IowaSeth M. Weinberg, University of PittsburghTerri H. Beaty, Johns Hopkins Bloomberg School of Public HealthEleanor Feingold, University of PittsburghJeffrey C. Murray, University of IowaMary L. Marazita, University of PittsburghElizabeth Leslie, Emory University
    Date:2017
    Publisher:Wiley: 12 months
    Publication Version:Author Accepted Manuscript (After Peer Review)